“…1) were synthesized by the Mallory–Katz photocyclization route from stilbene 3 obtained accordingly from (3-benzothienyl)methylphosphonate 4 and formylbenzo-18-crown-6 5 by the Horner–Wadsworth–Emmons reaction. Phosphonate 4 was synthesized from 3-methylbenzothiophene 6 by the bromination-Arbuzov reaction sequence (Scheme 1) As expected, a mixture of two products is formed, 31,32 which were isolated by column chromatography.…”
Two novel macrocyclic compounds with a crown ether moiety annulated to a tetracyclic thiophene-containing aromatic fragment were synthesized by the Mallory–Katz photocyclization reaction from a single stilbene precursor. These compounds...
“…1) were synthesized by the Mallory–Katz photocyclization route from stilbene 3 obtained accordingly from (3-benzothienyl)methylphosphonate 4 and formylbenzo-18-crown-6 5 by the Horner–Wadsworth–Emmons reaction. Phosphonate 4 was synthesized from 3-methylbenzothiophene 6 by the bromination-Arbuzov reaction sequence (Scheme 1) As expected, a mixture of two products is formed, 31,32 which were isolated by column chromatography.…”
Two novel macrocyclic compounds with a crown ether moiety annulated to a tetracyclic thiophene-containing aromatic fragment were synthesized by the Mallory–Katz photocyclization reaction from a single stilbene precursor. These compounds...
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